EP0219862B1 - Photosensitive member for elektrophotography - Google Patents
Photosensitive member for elektrophotography Download PDFInfo
- Publication number
- EP0219862B1 EP0219862B1 EP86114674A EP86114674A EP0219862B1 EP 0219862 B1 EP0219862 B1 EP 0219862B1 EP 86114674 A EP86114674 A EP 86114674A EP 86114674 A EP86114674 A EP 86114674A EP 0219862 B1 EP0219862 B1 EP 0219862B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- photoconductive
- photosensitive member
- layer
- charge carrier
- polyvinyl acetal
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0528—Macromolecular bonding materials
- G03G5/0532—Macromolecular bonding materials obtained by reactions only involving carbon-to-carbon unsatured bonds
- G03G5/0542—Polyvinylalcohol, polyallylalcohol; Derivatives thereof, e.g. polyvinylesters, polyvinylethers, polyvinylamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/48—Isomerisation; Cyclisation
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D129/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Coating compositions based on hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Coating compositions based on derivatives of such polymers
- C09D129/14—Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
Definitions
- the present invention relates to a photosensitive member for electrophotography, and more particularly to a photosensitive member having a photoconductive layer containing a new binder polymer.
- the photoconductive layers of photosensitive members for electrophotography were conventionally made from inorganic photoconductive materials such as selenium, cadmium sulfide, zinc oxide, etc.
- selenium not only needs to be recovered as a toxic material but also has poor heat resistance because it is crystallized by heat.
- Cadmium sulfide also needs to be recovered as a toxic material and has poor humidity resistance.
- zinc oxide it has poor humidity resistance and insufficient durability for repeated copying. Thus, efforts have been made to develop new photoconductive layers.
- organic photoconductive compounds simply referred to as "OPC” for use in photosensitive members for electrophotography, and their use has been growing from year to year.
- OPC organic photoconductive compounds
- the organic photoconductive compounds are superior to the inorganic counterparts in that the former is lighter, easier to form into films, easier to manufacture photosensitive members and even capable of providing transparent photosensitive members depending on the types thereof.
- organic photosensitive members for electrophotography composed of organic photoconductive compounds (referred to simply as “OPC photosensitive members") are inferior to the inorganic counterparts with respect to sensitivity and durability. Therefore, they have been used primarily in low-speed machines so far.
- binder polymers are required to provide good stability to particle dispersion, and polyvinyl butyral is commonly used as such a binder.
- polyvinyl butyral is commonly used as such a binder.
- polyesters, polycarbonates, polystyrene, etc. are efficient in the separation and injection of charge carriers, but they fail to disperse photoconductive particles stably, resulting in the agglomeration of most photoconductive particles.
- the dispersion stabilization treatment of such polymers leads to the decrease in sensitivity and electric properties such as residual potential, etc.
- binder polymers having not only satisfactory properties such as electric properties necessary for photosensitive members but also high adaptability for manufacturing photosensitive members have not been found yet.
- An object of the present invention is, therefore, to provide a photosensitive member for electrophotography having a photoconductive layer containing a polymer binder which not only can stably disperse photoconductive particles but also has excellent electric properties.
- the photosensitive member for electrophotography has a photoconductive layer on a conductive substrate, the photoconductive layer containing polyvinyl acetal having a constituent unit represented by the following general formula [I]: wherein Ar represents an aryl group; R1 a hydrogen atom, a lower alkyl group or an aryl group; and m an integer of 0 or 1-3, and a constituent unit represented by the following general formula [II]: wherein R2 represents a hydrogen atom or an acyl group, the constituent unit [I] being 40 mole % or more and the total of the constituent units [I] and [II] being 60 mole % or more.
- Ar represents an aryl group
- R1 a hydrogen atom, a lower alkyl group or an aryl group
- m an integer of 0 or 1-3
- R2 represents a hydrogen atom or an acyl group
- the constituent unit represented by the general formula [I] has an aryl group which may be a monovalent group derived from aromatic hydrocarbons such as benzene, styrene, stilbene, biphenyl, terphenyl, naphthalene, anthracene, acenaphthene, acenaphthylene, fluorene, phenanthrene, etc., which may be substituted.
- aromatic hydrocarbons such as benzene, styrene, stilbene, biphenyl, terphenyl, naphthalene, anthracene, acenaphthene, acenaphthylene, fluorene, phenanthrene, etc.
- the substituents of this aryl group may be lower alkyl groups such as methyl, ethyl and butyl; alkoxy groups such as methoxy and ethoxy; aryloxy groups such as phenoxy and tolyloxy; arylalkyl groups such as benzyl and naphthyl methyl; arylalkoxy groups such as benzyloxy; substituted amino groups such as dimethylamino, diethylamino, dibenzylamino and diphenylamino; halogen atoms such as chlorine and bromine; and a hydroxy group.
- alkyl groups such as methyl, ethyl and butyl
- alkoxy groups such as methoxy and ethoxy
- aryloxy groups such as phenoxy and tolyloxy
- arylalkyl groups such as benzyl and naphthyl methyl
- arylalkoxy groups such as benzyloxy
- substituted amino groups such as di
- the substituent R1 may be a hydrogen atom; a lower alkyl group such as methyl, ethyl, propyl and butyl; and the above-mentioned aryl group.
- the number "m” is an integer of 0 or 1-3.
- the substituent R2 is a hydrogen atom or an acyl group. It should be noted that in the polyvinyl acetal of the present invention containing a plurality of the constituent units [II], R2 may be a hydrogen atom for some of the constituent units [II] and an acry group for the rest.
- the acyl group represented by R2 may include a lower aliphatic acyl group such as acetyl and propionyl; and an aromatic acyl group such as benzoyl, anisyl carbonyl and naphthoyl.
- the polymer of the present invention contains 40 mole % or more, preferably 50 mole % or more of a monomer unit represented by the general formula [I], and the total of the monomer units [I] and [II] is 60 mole % or more, preferably 70 mole % or more.
- monomer units other than the above units [I] and [II] may be contained in the polymer in an amount of 40 mole % or less, preferably 30 mole % or less.
- Such other monomer units may include ethylene, styrene, methyl vinyl ether, etc.
- the polyvinyl acetal of the present invention may be prepared from aldehyde and alcohol by a known method.
- the alcohols which may be used include completely or partially saponified polyvinyl alcohols and their copolymers with various vinyl compounds.
- the aldehydes which may be used include aldehydes corresponding to the aldehyde moiety (pendant group) in the formula [I] and acetals such as dimethyl acetals and diethyl acetals derived from such aldehydes.
- the polyvinyl acetal of the present invention may be prepared from the above polyvinyl alcohol and the above aldehyde or its acetal in an organic solvent in the presence of an acid catalyst.
- the organic solvents which may be used include alcohols such as methanol, ethanol, propanol and 2-methoxyethanol; ethers such as tetrahydrofuran and dioxane; ketones such as methyl ethyl ketone and methylisobutyl ketone; aromatic hydrocarbons such as toluene, xylene and chlorobenzene; halogenated hydrocarbons such as chloroform, dichloroethane and trichloroethylene, polar aprotic solvents such as N,N-dimethyl formamide, acetonitrile, N-methyl pyrrolidone and sulfolane; and esters such as ethyl acetate, methyl benzoate and methyl cellosolve acetate. Mixtures of these solvents or their mixtures with water may also be used.
- the acids used as catalysts may be mineral acids such as hydrochloric acid and sulfuric acid, sulfonic acids such as p-toluene sulfonic acid and benzene sulfonic acid, etc.
- the reaction proceeds at room temperature, but the reaction mixture is usually heated to accelerate the reaction.
- the reaction temperature is desirably 40-100°C.
- the polyvinyl acetal of the present invention has not only good dispersion stability for photoconductive particles but also is highly effective in the separation and injection of charge carriers. In addition, it is highly soluble in organic solvents and has good compatibility with various photoconductive compounds. Accordingly, the polyvinyl acetal of the present invention can be used as a binder polymer for various types of photoconductive layers, which are enumerated as follows:
- the polyvinyl acetal of the present invention well ensures the stable dispersion of photoconductive particles and the separation and injection of charge carriers, it is particularly suitable as a binder polymer for the photoconductive layer having photoconductive particles dispersed therein and the charge carrier generating layer.
- a conductive substrate on which the photoconductive layer is to be formed may be any of those which can be used for conventional photosensitive members for electrophotography.
- the conductive substrates may be, for instance, metal drums or sheets made of aluminum, stainless steel, copper, etc., laminates having foils of such metal or deposited layers of such metal.
- Plastic films, plastic drums, papers, paper tubes, etc. coated with conductive mixtures of conductive materials such as metal powder, carbon black, copper iodide, polyelectrolytes, etc. and proper binders may also be used as the conductive substrates.
- sheets and drums of conductive plastics containing conductive materials such as metal powder, carbon black and carbon fibers may also be used.
- plastic films and belts treated to have conductivity by conductive metal oxides such as tin oxide, indium oxide, etc. are also usable.
- the photoconductive layer of any of the above types (1)-(4) is formed on such a conductive substrate, and if necessary, an undercoat, a bonding layer, a protective layer, a transparent, insulating layer, etc., may further be formed.
- the components which form the photoconductive layers may include photoconductive particles, organic photoconductive compounds, charge carrier transport media, sensitizers, binder polymers, plasticizers, antioxidants, ultraviolet light absorbers, etc., and a proper combination of these additives are used depending on the types of the photoconductive layers.
- the photoconductive particles used in combination with the polyvinyl acetal of the present invention are those generating charge carriers with high efficiency upon absorption of light.
- Typical examples of such photoconductive particles are inorganic, photoconductive particles of selenium, a selenium-tellurium alloy, a selenium-arsenic alloy, cadmium sulfide, zinc oxide, amorphous silicon, etc.; and organic, photoconductive particles of phthalocyanine pigments such as metal-free phthalocyanine, copper phthalocyanine, vanadyl phthalocyanine, aluminum phthalocyanine, titanyl phthalocyanine, indium phthalocyanine and magnesium phthalocyanine, perinone pigments, perylene pigments, anthraquinone pigments, polycyclic quinone pigments, azo pigments, quinacridone pigments, indigo pigments such as indigo and thioindigo, cyanine pigments, pyrylium salt pigments, thi
- photoconductive particles are dispersed in the polymer binder.
- the ratio of the photoconductive particles to the binder may vary depending upon the types of the photoconductive layers, but usually 10-2000 parts by weight, preferably 20-500 parts by weight of the binder is used per 100 parts by weight of the photoconductive particles.
- the binder may be composed of the polyvinyl acetal of the present invention alone, but it may contain other polymers.
- Such other binder polymers include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylates, methacrylates, vinyl alcohol and ethyl vinyl ether, other polyvinyl acetals, polycarbonates, polyesters, polyamides, polyurethanes, cellulose esters, cellulose ethers, phenoxy resins, silicone resins and epoxy resins.
- the organic photoconductive compounds and the charge carrier transport material in the photosensitive member according to the present invention are electron-donating compounds simply called electron donors and electron-attracting compounds simply called electron acceptors.
- the electron-donating compounds may be polymers having heterocyclic pendant groups or condensed polycyclic pendant groups such as poly-N-vinyl carbazole and polystyryl anthracene, and as low-molecular compounds, heterocyclic compounds such as pyrazoline, imidazole, oxazole, oxadiazole, triazole and carbazole, triaryl alkane derivatives such as triphenyl methane, triaryl amine derivatives such as triphenyl amine, phenylenediamine derivatives, N-phenyl carbazole derivatives, stilbene derivatives, hydrazone compounds, etc.
- the electron-attracting compounds may be trinitrofluorenone, tetranitrofluorenone, tetracyanoethylene, etc.
- These compounds may be used as charge carrier transport materials in layers having the photoconductive particles dispersed therein and in charge carrier transport layers in laminate-type photosensitive members, or may be used for photoconductive layers in which they are dissolved in polymer binders, if necessary, together with sensitizers such as dyes and electron-attracting compounds.
- sensitizers which include dyes which include triphenylmethane dyes such as Methyl Violet, Brilliant Green and Crystal Violet; thiazine dyes such as Methylene Blue; quinone dyes such as Quinizaline; and cyanine dyes as well as pyrylium salts, thiapyrylium salts and benzopyrylium salts, and electron-attracting compounds which include quinones such as chloranil, 2,3,-dichloro-1,4-naphthoquinone, 2-methylanthraquinone, 1-nitroanthraquinone, 1-chloro-5-nitroanthraquinone, 2-chloroanthraquinone and phenanthrenequinone; aldehydes such as 4-nitrobenzaldehyde; ketones such as 9-benzoylanthracene, indanedione, 3,5-dinitrobenzophenone, 2,4,7-trinitrofluorenone, 2,4,5,
- the polyvinyl acetal of the present invention may be used as binders not only in layers having the photoconductive particles dispersed therein, but also in the charge carrier transport layers and the photoconductive layers containing organic photoconductive compounds and sensitizers.
- the polyvinyl acetal of the present invention is added to the organic photoconductive compound or the charge carrier transport material, if necessary, together with the above polymers.
- the amount of the polyvinyl acetal may vary depending on whether the photoconductive compound is a high-molecular compound or a low-molecular compound.
- the photoconductive compound is a high-molecular compound such as polyvinyl carbazole
- the polyvinyl acetal of the present invention may be mixed in a small amount for improving the flexibility of the resulting photosensitive member.
- the photoconductive compound is a low-molecular compound
- a considerably large amount of the polyvinyl acetal should be used for a film-forming purpose.
- the photoconductive compound it is usually 10-200 parts by weight, preferably 30-150 parts by weight per 100 parts by weight of the binder containing the polyvinyl acetal, when the photoconductive compound is a low-molecular compound.
- the polyvinyl acetal of the present invention is suitable as a binder polymer particularly for those having the photoconductive layers having the photoconductive particles dispersed therein and those of the laminate type having the above photoconductive particle-dispersed layers as charge carrier generating layers.
- Fig. 1 Infrared spectrum was measured on this polymer in the form of a film. The result is shown in Fig. 1. As is apparent from Fig. 1, this is a polymer of acetal containing an aromatic ring.
- This coating fluid was applied by a film applicator to an aluminum vapor deposition layer formed on a 75- ⁇ m-thick polyester film so that the amount of the bisazo pigment coated was 0.25 g/m2, and then dried to provide a charge carrier generating layer.
- This charge carrier generating layer was coated with a 20- ⁇ m-thick charge carrier transport layer consisting of 90 parts of N-methyl-3-carbazolecarbaldehyde diphenylhydrazone represented by the following formula: 2 parts of 4-(p-nitrobenzoyloxy)benzalmalononitrile and 100 parts of a polycarbonate resin (NOVAREX 7025A manufactured by Mitsubishi Chemical Industries Ltd.) by coating to provide a photosensitive member for electrophotography.
- a 20- ⁇ m-thick charge carrier transport layer consisting of 90 parts of N-methyl-3-carbazolecarbaldehyde diphenylhydrazone represented by the following formula: 2 parts of 4-(p-nitrobenzoyloxy)benzalmalononitrile and 100 parts of a polycarbonate resin (NOVAREX 7025A manufactured by Mitsubishi Chemical Industries Ltd.) by coating to provide a photosensitive member for electrophotography.
- This photosensitive member was measured with respect to sensitivity which was expressed by half-decay exposure (E 1 2 ) by means of an electrophotographic paper test machine (Model SP-428 manufactured by Kawaguchi Denki Seisakusho K.K.). The measurement was carried out by giving a negative charge to the photosensitive member by corona discharge whose voltage was set to provide 22- ⁇ A corona current in the dark, and then exposing it to a tungsten lamp of 5 lux to determine the amount of light exposure (E 1 2 ) necessary for reducing the surface potential of the photosensitive member by half from -450V to -225V. As a result, the half-decay exposure of this photosensitive member was 0.7 lux ⁇ sec.
- the amount of light exposure consumed for reducing the surface potential to one-fifth from -450V to -90V was 1.3 lux ⁇ sec. After 10 seconds of exposure, the surface potential of the photosensitive member was sufficiently reduced and leveled off at -4V, which was residual potential.
- This photosensitive member was formed on an aluminum drum and tested with a plain paper copier (SF-8200 manufactured by Sharp Corp.). Since it had very high sensitivity, the test was performed with light exposure reduced by adjusting an exposure dial.
- Example 1 was repeated except for using Polyvinyl butyral (S'LEC B manufactured by Sekisui Chemical Co., Ltd.) instead of the polyvinyl acetal of Example 1 to produce a photosensitive member.
- Polyvinyl butyral S'LEC B manufactured by Sekisui Chemical Co., Ltd.
- This photosensitive member had sensitivity of 0.9 lux sec for E 1 2 and 1.7 lux ⁇ sec for E 1/5 and residual potential of -4V.
- Example 1 the polyvinyl acetal of the present invention used in Example 1 is superior to the conventional polyvinyl butyral not only in dispersion stability for pigments but also in enhancing the sensitivity of photosensitive members.
- Example 1 was repeated to produce a photosensitive member except for using instead of the bisazo pigment crystalline oxytitanium phthalocyanine showing an X-ray diffraction spectrum having no diffraction peaks at Bragg angles (2 ⁇ 0.2°) of 9 or less and strong diffraction peaks at Bragg angles of 9.3°, 10.6°, 13.2°, 15.1°, 15.7°, 16.1°, 20.7°, 23.3°, 26.2° and 27.1° as shown in Fig. 4.
- the charge carrier transport layer was prepared to have a thickness of 13 ⁇ m.
- the resulting photosensitiye member had sensitivity of 0.58 lux ⁇ sec for E 1 2 and 1.20 lux ⁇ sec for E 1/5 and residual potential of -7V.
- Example 2 The same procedures as in Example 2 were carried out to produce a photosensitive member except for using polyvinyl butyral used in Comparative Example 1 instead of the polyvinyl acetal of Example 2.
- the resulting photosensitive member had sensitivity of 0.70 lux sec for E 1 2 and 1.64 lux ⁇ sec for E 1/5 and residual potential of -17V.
- Example 2 shows that the polyvinyl acetal of the present invention is more effective not only for increasing sensitivity but also for reducing residual potential, which means that it is highly effective for the generation and injection of carriers in a laminate-type photosensitive member.
- Example 2 was repeated to produce photosensitive members except for using instead of the polyvinyl acetal of Example 2 polyvinyl acetal represented by the following general formula: wherein Ar, R1, m, p and q were as shown in Table 1. Incidentally, the values of p and q were determined by elemental analysis. Sensitivity was measured on each photosensitive member. The results are shown in Table 1.
- Example 9 The same procedures as in Example 9 were repeated to prepare a pigment dispersion-type photosensitive member except for using polyvinyl butyral in Comparative Example 1 instead of the polyvinyl acetal of Example 9. Sensitivity was measured in the same way as in Example 9. However, substantially no drop of surface potential by light exposure was observed under this measurement condition, making it. impossible to determine the sensitivity. This shows that the polyvinyl acetal of the present invention has excellent properties even when it is used in a pigment-dispersed photosensitive member containing no charge carrier transport medium.
- Example 1 was repeated to produce a photosensitive member for electrophotography except for using polyvinyl acetal made in Reference Example 1 as a binder for the charge carrier transport layer instead of the polycarbonate resin in Example 1.
- the resulting photosensitive member had sensitivity (E 1 2 ) of 0.9 lux ⁇ sec and residual potential of -8V.
- Example 10 was repeated to produce a photosensitive member except for using, instead of the polyvinyl acetal added to the charge carrier transport layer in Example 10, polyvinyl acetal represented by the following general formula: It was observed that the resulting photosensitive member had sensitivity (E 1 2 ) of 0.85 lux ⁇ sec and residual potential of -6V.
- Example 9 0.5 part of 4-diethylaminobenzaldehyde diphenylhydrazone was dissolved in the oxytitanium phthalocyanine-dispersed coating fluid prepared in Example 9, and then coating and drying were carried out in the same way as in Example 9 to produce a photosensitive member having a pigment-dispersed layer. It was observed that the photosensitive layer had sensitivity (E 1 2 ) of 0.70 lux ⁇ sec and residual potential of +4V.
- the polyvinyl acetal of the present invention has not only good dispersion stability for photoconductive particles but also good compatibility with various photoconductive compounds. Accordingly, it facilitates the formation of photosensitive members, and also it is superior to conventional binder polymers with respect to the separation and injection of charge carriers. Therefore, the use of such polyvinyl acetal provides the photosensitive members having higher sensitivity and lower residual potential than the conventional ones. In addition, the photosensitive members containing this polyvinyl acetal enjoy higher durability.
Description
- The present invention relates to a photosensitive member for electrophotography, and more particularly to a photosensitive member having a photoconductive layer containing a new binder polymer.
- The photoconductive layers of photosensitive members for electrophotography were conventionally made from inorganic photoconductive materials such as selenium, cadmium sulfide, zinc oxide, etc. However, selenium not only needs to be recovered as a toxic material but also has poor heat resistance because it is crystallized by heat. Cadmium sulfide also needs to be recovered as a toxic material and has poor humidity resistance. As for zinc oxide, it has poor humidity resistance and insufficient durability for repeated copying. Thus, efforts have been made to develop new photoconductive layers.
- Recently, research has been advanced on organic photoconductive compounds simply referred to as "OPC" for use in photosensitive members for electrophotography, and their use has been growing from year to year. The organic photoconductive compounds are superior to the inorganic counterparts in that the former is lighter, easier to form into films, easier to manufacture photosensitive members and even capable of providing transparent photosensitive members depending on the types thereof.
- Despite these advantages, the organic photosensitive members for electrophotography composed of organic photoconductive compounds (referred to simply as "OPC photosensitive members") are inferior to the inorganic counterparts with respect to sensitivity and durability. Therefore, they have been used primarily in low-speed machines so far.
- To improve the sensitivity and durability of the OPC photosensitive members, research has been carried out vigorously to develop new charge carrier generating materials, photoconductive compounds such as charge carrier transport materials, sensitizers, etc. On the contrary, binder polymers have not been well investigated so far despite the fact that they largely affect the properties of the resulting photosensitive members. As a matter of fact, most of the OPC photosensitive members practically used at present employ commercially available general-purpose polymers. Selection among a lot of commercially available polymers is made from the viewpoint of photosensitive properties and easiness to production. Accordingly, these binder polymers are not necessarily suitable for having the photoconductive compounds fully exhibit their own properties. For instance, in such photosensitive members as having photoconductive particles dispersed therein, binder polymers are required to provide good stability to particle dispersion, and polyvinyl butyral is commonly used as such a binder. However, it is poor in the separation and injection of charge carriers and suffers from such problems as sensitivity decrease and residual potential increase. On the other hand, polyesters, polycarbonates, polystyrene, etc. are efficient in the separation and injection of charge carriers, but they fail to disperse photoconductive particles stably, resulting in the agglomeration of most photoconductive particles. Further, the dispersion stabilization treatment of such polymers leads to the decrease in sensitivity and electric properties such as residual potential, etc.
- Thus, binder polymers having not only satisfactory properties such as electric properties necessary for photosensitive members but also high adaptability for manufacturing photosensitive members have not been found yet.
- An object of the present invention is, therefore, to provide a photosensitive member for electrophotography having a photoconductive layer containing a polymer binder which not only can stably disperse photoconductive particles but also has excellent electric properties.
- Intense research has led to the finding that the above object can be achieved by using as a binder polymer a new polyvinyl acetal having not only excellent stability for the dispersion of photoconductive particles but also excellent electric properties. The present invention is based on this finding.
- That is, the photosensitive member for electrophotography according to the present invention has a photoconductive layer on a conductive substrate, the photoconductive layer containing polyvinyl acetal having a constituent unit represented by the following general formula [I]:
wherein Ar represents an aryl group; R₁ a hydrogen atom, a lower alkyl group or an aryl group; and m an integer of 0 or 1-3, and
a constituent unit represented by the following general formula [II]:
wherein R₂ represents a hydrogen atom or an acyl group, the constituent unit [I] being 40 mole % or more and the total of the constituent units [I] and [II] being 60 mole % or more. -
- Figs. 1-3 are graphs showing infrared spectra of the polymers prepared in Reference Examples 1-3, respectively; and
- Fig. 4 is a graph showing an X-ray diffraction spectrum of oxytitanium phthalocyanine used in Example 2.
-
- In the polyvinyl acetal according to the present invention, the constituent unit represented by the general formula [I] has an aryl group which may be a monovalent group derived from aromatic hydrocarbons such as benzene, styrene, stilbene, biphenyl, terphenyl, naphthalene, anthracene, acenaphthene, acenaphthylene, fluorene, phenanthrene, etc., which may be substituted. The substituents of this aryl group may be lower alkyl groups such as methyl, ethyl and butyl; alkoxy groups such as methoxy and ethoxy; aryloxy groups such as phenoxy and tolyloxy; arylalkyl groups such as benzyl and naphthyl methyl; arylalkoxy groups such as benzyloxy; substituted amino groups such as dimethylamino, diethylamino, dibenzylamino and diphenylamino; halogen atoms such as chlorine and bromine; and a hydroxy group.
- The substituent R₁ may be a hydrogen atom; a lower alkyl group such as methyl, ethyl, propyl and butyl; and the above-mentioned aryl group.
- The number "m" is an integer of 0 or 1-3.
- In the constituent unit [II], the substituent R₂ is a hydrogen atom or an acyl group. It should be noted that in the polyvinyl acetal of the present invention containing a plurality of the constituent units [II], R₂ may be a hydrogen atom for some of the constituent units [II] and an acry group for the rest.
- The acyl group represented by R₂ may include a lower aliphatic acyl group such as acetyl and propionyl; and an aromatic acyl group such as benzoyl, anisyl carbonyl and naphthoyl.
- The polymer of the present invention contains 40 mole % or more, preferably 50 mole % or more of a monomer unit represented by the general formula [I], and the total of the monomer units [I] and [II] is 60 mole % or more, preferably 70 mole % or more. In other words, monomer units other than the above units [I] and [II] may be contained in the polymer in an amount of 40 mole % or less, preferably 30 mole % or less. Such other monomer units may include ethylene, styrene, methyl vinyl ether, etc.
- The polyvinyl acetal of the present invention may be prepared from aldehyde and alcohol by a known method.
- The alcohols which may be used include completely or partially saponified polyvinyl alcohols and their copolymers with various vinyl compounds. And the aldehydes which may be used include aldehydes corresponding to the aldehyde moiety (pendant group) in the formula [I] and acetals such as dimethyl acetals and diethyl acetals derived from such aldehydes.
- The polyvinyl acetal of the present invention may be prepared from the above polyvinyl alcohol and the above aldehyde or its acetal in an organic solvent in the presence of an acid catalyst.
- The organic solvents which may be used include alcohols such as methanol, ethanol, propanol and 2-methoxyethanol; ethers such as tetrahydrofuran and dioxane; ketones such as methyl ethyl ketone and methylisobutyl ketone; aromatic hydrocarbons such as toluene, xylene and chlorobenzene; halogenated hydrocarbons such as chloroform, dichloroethane and trichloroethylene, polar aprotic solvents such as N,N-dimethyl formamide, acetonitrile, N-methyl pyrrolidone and sulfolane; and esters such as ethyl acetate, methyl benzoate and methyl cellosolve acetate. Mixtures of these solvents or their mixtures with water may also be used.
- The acids used as catalysts may be mineral acids such as hydrochloric acid and sulfuric acid, sulfonic acids such as p-toluene sulfonic acid and benzene sulfonic acid, etc.
- The reaction proceeds at room temperature, but the reaction mixture is usually heated to accelerate the reaction. The reaction temperature is desirably 40-100°C.
- The polyvinyl acetal of the present invention has not only good dispersion stability for photoconductive particles but also is highly effective in the separation and injection of charge carriers. In addition, it is highly soluble in organic solvents and has good compatibility with various photoconductive compounds. Accordingly, the polyvinyl acetal of the present invention can be used as a binder polymer for various types of photoconductive layers, which are enumerated as follows:
- (1)
- A photoconductive layer having photoconductive particles dispersed in a binder.
- (2)
- A photoconductive layer of the above type (1) further containing a charge carrier transport material.
- (3)
- A photoconductive layer containing an organic photoconductive compound, a sensitizer and a polymer binder.
- (4)
- A photoconductive layer of a laminate type having a charge carrier generating layer and a charge carrier transport layer.
- Since the polyvinyl acetal of the present invention well ensures the stable dispersion of photoconductive particles and the separation and injection of charge carriers, it is particularly suitable as a binder polymer for the photoconductive layer having photoconductive particles dispersed therein and the charge carrier generating layer.
- Next, the photosensitive member for electrophotography according to the present invention will be explained in detail.
- A conductive substrate on which the photoconductive layer is to be formed may be any of those which can be used for conventional photosensitive members for electrophotography. Specifically, the conductive substrates may be, for instance, metal drums or sheets made of aluminum, stainless steel, copper, etc., laminates having foils of such metal or deposited layers of such metal. Plastic films, plastic drums, papers, paper tubes, etc. coated with conductive mixtures of conductive materials such as metal powder, carbon black, copper iodide, polyelectrolytes, etc. and proper binders may also be used as the conductive substrates. Further, sheets and drums of conductive plastics containing conductive materials such as metal powder, carbon black and carbon fibers may also be used. In addition to the above, plastic films and belts treated to have conductivity by conductive metal oxides such as tin oxide, indium oxide, etc. are also usable.
- The photoconductive layer of any of the above types (1)-(4) is formed on such a conductive substrate, and if necessary, an undercoat, a bonding layer, a protective layer, a transparent, insulating layer, etc., may further be formed.
- The components which form the photoconductive layers may include photoconductive particles, organic photoconductive compounds, charge carrier transport media, sensitizers, binder polymers, plasticizers, antioxidants, ultraviolet light absorbers, etc., and a proper combination of these additives are used depending on the types of the photoconductive layers.
- The photoconductive particles used in combination with the polyvinyl acetal of the present invention are those generating charge carriers with high efficiency upon absorption of light. Typical examples of such photoconductive particles are inorganic, photoconductive particles of selenium, a selenium-tellurium alloy, a selenium-arsenic alloy, cadmium sulfide, zinc oxide, amorphous silicon, etc.; and organic, photoconductive particles of phthalocyanine pigments such as metal-free phthalocyanine, copper phthalocyanine, vanadyl phthalocyanine, aluminum phthalocyanine, titanyl phthalocyanine, indium phthalocyanine and magnesium phthalocyanine, perinone pigments, perylene pigments, anthraquinone pigments, polycyclic quinone pigments, azo pigments, quinacridone pigments, indigo pigments such as indigo and thioindigo, cyanine pigments, pyrylium salt pigments, thiapyrylium salt pigments, squarylium pigments, etc.
- These photoconductive particles are dispersed in the polymer binder. The ratio of the photoconductive particles to the binder may vary depending upon the types of the photoconductive layers, but usually 10-2000 parts by weight, preferably 20-500 parts by weight of the binder is used per 100 parts by weight of the photoconductive particles.
- The binder may be composed of the polyvinyl acetal of the present invention alone, but it may contain other polymers. Such other binder polymers include polymers and copolymers of vinyl compounds such as styrene, vinyl acetate, vinyl chloride, acrylates, methacrylates, vinyl alcohol and ethyl vinyl ether, other polyvinyl acetals, polycarbonates, polyesters, polyamides, polyurethanes, cellulose esters, cellulose ethers, phenoxy resins, silicone resins and epoxy resins.
- Usable as the organic photoconductive compounds and the charge carrier transport material in the photosensitive member according to the present invention are electron-donating compounds simply called electron donors and electron-attracting compounds simply called electron acceptors. The electron-donating compounds may be polymers having heterocyclic pendant groups or condensed polycyclic pendant groups such as poly-N-vinyl carbazole and polystyryl anthracene, and as low-molecular compounds, heterocyclic compounds such as pyrazoline, imidazole, oxazole, oxadiazole, triazole and carbazole, triaryl alkane derivatives such as triphenyl methane, triaryl amine derivatives such as triphenyl amine, phenylenediamine derivatives, N-phenyl carbazole derivatives, stilbene derivatives, hydrazone compounds, etc. The electron-attracting compounds may be trinitrofluorenone, tetranitrofluorenone, tetracyanoethylene, etc.
- These compounds may be used as charge carrier transport materials in layers having the photoconductive particles dispersed therein and in charge carrier transport layers in laminate-type photosensitive members, or may be used for photoconductive layers in which they are dissolved in polymer binders, if necessary, together with sensitizers such as dyes and electron-attracting compounds.
- Typical examples of the sensitizers which may be used are dyes which include triphenylmethane dyes such as Methyl Violet, Brilliant Green and Crystal Violet; thiazine dyes such as Methylene Blue; quinone dyes such as Quinizaline; and cyanine dyes as well as pyrylium salts, thiapyrylium salts and benzopyrylium salts, and electron-attracting compounds which include quinones such as chloranil, 2,3,-dichloro-1,4-naphthoquinone, 2-methylanthraquinone, 1-nitroanthraquinone, 1-chloro-5-nitroanthraquinone, 2-chloroanthraquinone and phenanthrenequinone; aldehydes such as 4-nitrobenzaldehyde; ketones such as 9-benzoylanthracene, indanedione, 3,5-dinitrobenzophenone, 2,4,7-trinitrofluorenone, 2,4,5,7-tetranitrofluorenone and 3,3',5,5'-tetranitrobenzophenone; acid anhydrides such as phthalic anhydride and 4-chloronaphthalic anhydride; cyano compounds such as tetracyanoethylene, terephthalmalononitrile, 9-anthrylmethylidenemalononitrile, 4-nitrobenzalmalononitrile and 4-(p-nitrobenzoyloxy)benzalmalononitrile; phthalides such as 3-benzalphthalide, 3-(α-cyano-p-nitrobenzal)phthalide and 3-(α-cyano-p-nitrobenzal)-4,5,6,7-tetrachlorophthalide, etc.
- The polyvinyl acetal of the present invention may be used as binders not only in layers having the photoconductive particles dispersed therein, but also in the charge carrier transport layers and the photoconductive layers containing organic photoconductive compounds and sensitizers.
- The polyvinyl acetal of the present invention is added to the organic photoconductive compound or the charge carrier transport material, if necessary, together with the above polymers. The amount of the polyvinyl acetal may vary depending on whether the photoconductive compound is a high-molecular compound or a low-molecular compound. When the photoconductive compound is a high-molecular compound such as polyvinyl carbazole, the polyvinyl acetal of the present invention may be mixed in a small amount for improving the flexibility of the resulting photosensitive member. On the other hand, when the photoconductive compound is a low-molecular compound, a considerably large amount of the polyvinyl acetal should be used for a film-forming purpose. Incidentally, with respect to the photoconductive compound, it is usually 10-200 parts by weight, preferably 30-150 parts by weight per 100 parts by weight of the binder containing the polyvinyl acetal, when the photoconductive compound is a low-molecular compound.
- Among the photosensitive members for electrophotography having various structures and compositions as explained above, the polyvinyl acetal of the present invention is suitable as a binder polymer particularly for those having the photoconductive layers having the photoconductive particles dispersed therein and those of the laminate type having the above photoconductive particle-dispersed layers as charge carrier generating layers.
- The present invention will be explained in further detail by the following Examples. It should be noted, however, that they are not intended to limit the scope of the present invention. The term "part(s)" used in Examples means "part(s) by weight" unless specifically indicated otherwise.
- 10.0 parts of polyvinyl alcohol having a saponification ratio of 99.0-100 mole % (GOHSENOL NM-11 manufactured by the Nippon Synthetic Chemical Industry Co., Ltd.) was suspended in 250 parts of 1,2-dichlorethane, and 39 parts of phenylacetaldehyde and one part of concentrated hydrochloric acid were added thereto. The resulting reaction mixture was stirred while heating at 55°C for 5 hours. The reaction solution was poured into 1500 parts of methanol in which 1.5 parts of sodium acetate was dissolved to precipitate the resulting polyvinyl acetal. The polymer thus obtained was dissolved in tetrahydrofuran and precipitated again in methanol, and such purification procedures were repeated several times to remove the unreacted phenylacetaldehyde. Thus, 18.5 parts of a transparent, solid polymer was obtained.
- The elemental analysis of this polymer provided the following results:
Elemental Analysis C H Measured 74.24% 7.42% Calculated 74.24% 7.54% -
- As is apparent from the above results, the measured values of carbon and hydrogen percentages in the polymer well coincide with the values calculated from the general formula [III].
- Infrared spectrum was measured on this polymer in the form of a film. The result is shown in Fig. 1. As is apparent from Fig. 1, this is a polymer of acetal containing an aromatic ring.
- An acetal ratio defined by the formula:
-
- The procedures of Reference Example 1 were repeated except for using 41 parts of β-phenylpropionaldehyde instead of phenylacetaldehyde. As a result, 18.5 parts of a polymer was obtained.
- This polymer was subjected to elemental analysis. The results are as follows:
Elemental Analysis C H Measured 74.99% 7.95% Calculated 74.99% 7.98% -
- As is apparent from the above results, the measured values well coincide with the values calculated from the formula [IV].
- Infrared spectrum was measured on a film of this polymer formed on an NaCl plate. The results are shown in Fig. 2.
- The procedures of Reference Example 1 were repeated except for using 70 parts of p-tolylacetaldehyde dimethyl acetal instead of phenylacetaldehyde. As a result, 18 parts of a polymer was obtained.
- This polymer was subjected to elemental analysis. The results are as follows:
Elemental Analysis C H Measured 74.78% 8.11% Calculated 74.78% 7.99% -
- The measured values of carbon and hydrogen percentages in the polymer well coincide with the values calculated from the formula [V].
- Infrared spectrum was measured on a film of this polymer formed on an NaCl plate. The results are shown in Fig. 3.
-
- This coating fluid was applied by a film applicator to an aluminum vapor deposition layer formed on a 75-µm-thick polyester film so that the amount of the bisazo pigment coated was 0.25 g/m², and then dried to provide a charge carrier generating layer.
- This charge carrier generating layer was coated with a 20-µm-thick charge carrier transport layer consisting of 90 parts of N-methyl-3-carbazolecarbaldehyde diphenylhydrazone represented by the following formula:
2 parts of 4-(p-nitrobenzoyloxy)benzalmalononitrile and 100 parts of a polycarbonate resin (NOVAREX 7025A manufactured by Mitsubishi Chemical Industries Ltd.) by coating to provide a photosensitive member for electrophotography. - This photosensitive member was measured with respect to sensitivity which was expressed by half-decay exposure (
E E - This photosensitive member was formed on an aluminum drum and tested with a plain paper copier (SF-8200 manufactured by Sharp Corp.). Since it had very high sensitivity, the test was performed with light exposure reduced by adjusting an exposure dial.
- As a result, even after 20,000 copying the decrease in an image concentration was not observed, and extremely good copies were obtained without fogging. This means that this photosensitive member has extremely high durability.
- Example 1 was repeated except for using Polyvinyl butyral (S'LEC B manufactured by Sekisui Chemical Co., Ltd.) instead of the polyvinyl acetal of Example 1 to produce a photosensitive member.
-
- It is thus evident that the polyvinyl acetal of the present invention used in Example 1 is superior to the conventional polyvinyl butyral not only in dispersion stability for pigments but also in enhancing the sensitivity of photosensitive members.
- Example 1 was repeated to produce a photosensitive member except for using instead of the bisazo pigment crystalline oxytitanium phthalocyanine showing an X-ray diffraction spectrum having no diffraction peaks at Bragg angles (2ϑ±0.2°) of 9 or less and strong diffraction peaks at Bragg angles of 9.3°, 10.6°, 13.2°, 15.1°, 15.7°, 16.1°, 20.7°, 23.3°, 26.2° and 27.1° as shown in Fig. 4. The charge carrier transport layer was prepared to have a thickness of 13 µm.
-
- Incidentally, the above oxytitanium phthalocyanine was prepared by the following method:
- First, 97.5g of phthalodinitrile was added to 750ml of α-chloronaphthalene, and 22ml of titanium tetrachloride was dropped thereinto in a nitrogen atmosphere. After the completion of dropping, the reaction mixture was heated to temperatures of 200-220°C at which a reaction was caused to take place while stirring for 3 hours. It was then left to cool, and filtered at temperatures of 100-130°C, and then washed with 200ml of α-chloronaphthalene heated at 100°C. The resulting cake was washed in suspension with 300ml of α-chloronaphthalene and then with 300ml of methanol at room temperature. It was further subjected to washing in suspension with 800ml of hot methanol for one hour several times. The cake was then suspended in 700ml of hot water and washed for 2 hours. The resulting filtrate had pH of 1 or less. Washing in suspension with hot water was repeated until the pH of the filtrate became 6-7. Then, It was subjected to two-hour washing in suspension with 700ml of N-methyl pyrrolidone (manufactured by Mitsubishi Chemical Industries Ltd.) at 140-145°C four times. Finally, washing in suspension with 800ml of hot methanol was carried out twice to obtain the above oxytitanium phthalocyanine.
-
- The same procedures as in Example 2 were carried out to produce a photosensitive member except for using polyvinyl butyral used in Comparative Example 1 instead of the polyvinyl acetal of Example 2.
-
- The comparison with Example 2 shows that the polyvinyl acetal of the present invention is more effective not only for increasing sensitivity but also for reducing residual potential, which means that it is highly effective for the generation and injection of carriers in a laminate-type photosensitive member.
- Example 2 was repeated to produce photosensitive members except for using instead of the polyvinyl acetal of Example 2 polyvinyl acetal represented by the following general formula:
wherein Ar, R₁, m, p and q were as shown in Table 1. Incidentally, the values of p and q were determined by elemental analysis. Sensitivity was measured on each photosensitive member. The results are shown in Table 1. - 1 part of oxytitanium phthalocyanine used in
Exmaple 2 and 1 part of polyvinyl acetal produced in Reference Example 2 were pulverized to fine particles by a sand grinder in 80 parts of tetrahydrofuran to prepare a coating fluid. This coating fluid was applied by a film applicator onto an aluminum vapor deposition layer formed on a 75-µm-thick polyester film to form an oxytitanium phthalocyanine-dispersed layer having a thickness of 10µm after drying. The photosensitive member thus prepared was given a positive charge with corona discharge in a dark place and measured with respect to sensitivity. As a result, the half-decay exposure (E - The same procedures as in Example 9 were repeated to prepare a pigment dispersion-type photosensitive member except for using polyvinyl butyral in Comparative Example 1 instead of the polyvinyl acetal of Example 9. Sensitivity was measured in the same way as in Example 9. However, substantially no drop of surface potential by light exposure was observed under this measurement condition, making it. impossible to determine the sensitivity. This shows that the polyvinyl acetal of the present invention has excellent properties even when it is used in a pigment-dispersed photosensitive member containing no charge carrier transport medium.
- Example 1 was repeated to produce a photosensitive member for electrophotography except for using polyvinyl acetal made in Reference Example 1 as a binder for the charge carrier transport layer instead of the polycarbonate resin in Example 1. The resulting photosensitive member had sensitivity (
E - After charging and exposing were repeated 2,000 times by the above test machine, it was observed that the surface potential of the photosensitive member was 99.7% of the initial level, which means that the surface potential is extremely stable.
- Example 10 was repeated to produce a photosensitive member except for using, instead of the polyvinyl acetal added to the charge carrier transport layer in Example 10, polyvinyl acetal represented by the following general formula:
It was observed that the resulting photosensitive member had sensitivity (E - 0.5 part of 4-diethylaminobenzaldehyde diphenylhydrazone was dissolved in the oxytitanium phthalocyanine-dispersed coating fluid prepared in Example 9, and then coating and drying were carried out in the same way as in Example 9 to produce a photosensitive member having a pigment-dispersed layer. It was observed that the photosensitive layer had sensitivity (
E - As explained above, the polyvinyl acetal of the present invention has not only good dispersion stability for photoconductive particles but also good compatibility with various photoconductive compounds. Accordingly, it facilitates the formation of photosensitive members, and also it is superior to conventional binder polymers with respect to the separation and injection of charge carriers. Therefore, the use of such polyvinyl acetal provides the photosensitive members having higher sensitivity and lower residual potential than the conventional ones. In addition, the photosensitive members containing this polyvinyl acetal enjoy higher durability.
- The present invention has been explained specifically above, but it should be noted that any modifications can be made unless they deviate from the scope of the present invention which is defined by the claims attached hereto.
Claims (6)
- A photosensitive member for electrophotography comprising at least a photoconductive layer on a conductive substrate, said photoconductive layer containing polyvinyl acetal having a constituent unit represented by the following general formula [I]:
and a constituent unit represented by the following general formula [II]: - The photosensitive member for electrophotography according to claim 1, wherein said photoconductive layer has photoconductive particles dispersed in a binder.
- The photosensitive member for electrophotography according to claim 2, wherein said photoconductive layer contains a charge carrier transport medium.
- The photosensitive member for electrophotography according to claim 1, wherein said photoconductive layer contains an organic photoconductive compound, a sensitizer and a polymer binder.
- The photosensitive member for electrophotography according to claim 1, wherein said photoconductive layer is a laminate composed of a charge carrier generating layer and a charge carrier transport layer, and said polyvinyl acetal is contained as a binder polymer in said charge carrier generating layer.
- The photosensitive layer for electrophotography according to claim 1, wherein said photoconductive member is a laminate composed of a charge carrier generating layer and a charge carrier transport layer, and said polyvinyl acetal is contained in said charge carrier transport layer.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP236964/85 | 1985-10-23 | ||
JP60236964A JPH0746227B2 (en) | 1985-10-23 | 1985-10-23 | Electrophotographic photoconductor |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0219862A2 EP0219862A2 (en) | 1987-04-29 |
EP0219862A3 EP0219862A3 (en) | 1990-01-10 |
EP0219862B1 true EP0219862B1 (en) | 1993-03-31 |
Family
ID=17008374
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86114674A Expired - Lifetime EP0219862B1 (en) | 1985-10-23 | 1986-10-22 | Photosensitive member for elektrophotography |
Country Status (4)
Country | Link |
---|---|
US (1) | US4734348A (en) |
EP (1) | EP0219862B1 (en) |
JP (1) | JPH0746227B2 (en) |
DE (1) | DE3688173T2 (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0715588B2 (en) * | 1987-06-03 | 1995-02-22 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor |
JPS63303361A (en) * | 1987-06-03 | 1988-12-09 | Fuji Xerox Co Ltd | Electrophotographic sensitive body |
US4898799A (en) * | 1987-07-10 | 1990-02-06 | Konica Corporation | Photoreceptor |
JP2718044B2 (en) * | 1988-01-07 | 1998-02-25 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor |
JP2653076B2 (en) * | 1988-01-07 | 1997-09-10 | 富士ゼロックス株式会社 | Electrophotographic photoreceptor |
US5066633A (en) * | 1990-02-09 | 1991-11-19 | Graphic Controls Corporation | Sensitizer for heat sensitive paper coatings |
US5288575A (en) * | 1991-11-14 | 1994-02-22 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, and electrophotographic apparatus, device unit and facsimile machine employing the photosensitive member |
US5320923A (en) * | 1993-01-28 | 1994-06-14 | Hewlett-Packard Company | Reusable, positive-charging organic photoconductor containing phthalocyanine pigment, hydroxy binder and silicon stabilizer |
US5654902A (en) * | 1993-05-03 | 1997-08-05 | Sony Deutschland Gmbh | Recyclable component with data storage for storing information for examining the component and product including such a component |
DE69531122T2 (en) * | 1994-03-25 | 2004-05-19 | Hewlett-Packard Co., Palo Alto | Polymeric binders with saturated ring units for positively charged, organic single-layer photoreceptors |
US5750300A (en) * | 1996-04-18 | 1998-05-12 | Hewlett-Packard Company | Photoconductor comprising a complex between metal oxide phthalocyanine compounds and hydroxy compounds |
JP3798112B2 (en) * | 1996-04-30 | 2006-07-19 | ヒューレット・パッカード・カンパニー | Low temperature curing binder |
US7186490B1 (en) * | 1999-05-06 | 2007-03-06 | Ricoh Company, Ltd. | Photosensitive material, electrophotographic photoreceptor using the material, and electrophotographic image forming method and apparatus using the photoreceptor |
US6489070B1 (en) | 2001-03-09 | 2002-12-03 | Lexmark International, Inc. | Photoconductors comprising cyclic carbonate polymers |
JP3907112B2 (en) * | 2002-06-28 | 2007-04-18 | 株式会社リコー | Electrophotographic photosensitive member, method for producing electrophotographic photosensitive member, and image forming apparatus |
EP2264539B1 (en) * | 2004-05-27 | 2012-03-21 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus |
US8088541B2 (en) | 2005-12-07 | 2012-01-03 | Canon Kabushiki Kaisha | Polyvinyl acetal resin, electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus |
JP5585668B2 (en) * | 2011-02-15 | 2014-09-10 | 富士電機株式会社 | Electrophotographic photoreceptor, method for producing the same, and electrophotographic apparatus |
WO2012111099A1 (en) * | 2011-02-15 | 2012-08-23 | 富士電機株式会社 | Electrophotographic photosensitive body, method for producing same, and electrophotographic device |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5033858B2 (en) * | 1972-02-01 | 1975-11-04 | ||
US4259425A (en) * | 1979-05-11 | 1981-03-31 | Monsanto Company | Electrographic recording material |
DE3024772A1 (en) * | 1980-06-30 | 1982-01-28 | Hoechst Ag, 6000 Frankfurt | ELASTIC, LAMINATE LIGHT SENSITIVE LAYER |
NL8100163A (en) * | 1981-01-15 | 1982-08-02 | Oce Nederland Bv | REPEATEDLY USABLE ELECTROPHOTOGRAPHIC ELEMENT AND METHOD FOR MANUFACTURING THAT ELEMENT. |
JPS61149964A (en) * | 1984-12-25 | 1986-07-08 | Canon Inc | Electrophotographic sensitive body |
-
1985
- 1985-10-23 JP JP60236964A patent/JPH0746227B2/en not_active Expired - Fee Related
-
1986
- 1986-10-17 US US06/920,728 patent/US4734348A/en not_active Expired - Lifetime
- 1986-10-22 EP EP86114674A patent/EP0219862B1/en not_active Expired - Lifetime
- 1986-10-22 DE DE86114674T patent/DE3688173T2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH0746227B2 (en) | 1995-05-17 |
EP0219862A2 (en) | 1987-04-29 |
EP0219862A3 (en) | 1990-01-10 |
DE3688173T2 (en) | 1993-10-21 |
JPS6295537A (en) | 1987-05-02 |
US4734348A (en) | 1988-03-29 |
DE3688173D1 (en) | 1993-05-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0219862B1 (en) | Photosensitive member for elektrophotography | |
US4367273A (en) | Electrophotographic plate comprising a conductive substrate and a photosensitive layer containing an organic photoconductor layer composed of a hydrazone compound | |
US5080991A (en) | Electrophotographic photoreceptor with a hydrazone | |
US5134048A (en) | Electrophotographic recording material containing photoconductive porphyrin compounds | |
EP0353067B1 (en) | Electrophotographic photosensitive material containing m-phenylenediamine compound | |
JP3042044B2 (en) | Electrophotographic photoreceptor | |
US6117604A (en) | Phthalocyanine compound and organic photoconductor | |
US4396694A (en) | Organic electrophotographic sensitive materials | |
JPH026484A (en) | 1,2,4,5-benzoylene(naphtho(1,8-de)pyrimidine) compound and use thereof | |
US4987045A (en) | Photosensitive member for electrophotography | |
JP2814586B2 (en) | Electrophotographic photoreceptor | |
JPH09138512A (en) | Electrophotographic photoreceptor | |
JPH05100456A (en) | Electrophotographic sensitive body | |
JP3570081B2 (en) | Electrophotographic photoreceptor | |
JPH04321649A (en) | Bisstyryl compound, phosphorous acid compound and electrophotographic sensitized material | |
JP2808763B2 (en) | Electrophotographic photoreceptor | |
EP0226751B1 (en) | Photosensitive member for electrophotography | |
US5932382A (en) | Phthalocyanine compound and electrophotographic photoreceptor comprising same | |
JP3810169B2 (en) | Electrophotographic photoreceptor | |
JP3576908B2 (en) | Electrophotographic photoreceptor | |
US6008346A (en) | Phthalocyanine compound and electrophotographic photoreceptor comprising same | |
EP0232854A2 (en) | Electrophotographic photoreceptor | |
JPH11352709A (en) | Electrophotographic photoreceptor | |
JPS6317456A (en) | Electrophotographic sensitive body | |
JPS61121058A (en) | Electrophotographic sensitive body |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A2 Designated state(s): BE CH DE ES FR GB IT LI NL |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: MITSUBISHI KASEI CORPORATION |
|
PUAL | Search report despatched |
Free format text: ORIGINAL CODE: 0009013 |
|
AK | Designated contracting states |
Kind code of ref document: A3 Designated state(s): BE CH DE ES FR GB IT LI NL |
|
17P | Request for examination filed |
Effective date: 19900508 |
|
17Q | First examination report despatched |
Effective date: 19920604 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): BE CH DE ES FR GB IT LI NL |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 19930331 Ref country code: BE Effective date: 19930331 Ref country code: LI Effective date: 19930331 Ref country code: NL Effective date: 19930331 Ref country code: CH Effective date: 19930331 |
|
REF | Corresponds to: |
Ref document number: 3688173 Country of ref document: DE Date of ref document: 19930506 |
|
ET | Fr: translation filed | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 19930712 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
NLV1 | Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19971231 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19980915 Year of fee payment: 13 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19980930 Year of fee payment: 13 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19991022 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19991022 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20000630 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20000801 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |